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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13655Erstellt: 24. Oktober 2026

1-(Methylsulphonyl)acetone → 6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinoline

https://huagongshe.com/de/reaction/13655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Methylsulphonyl)acetoneHCID 78695—
Edukt2-Amino-5-bromobenzophenoneHCID 99677—
EduktSodiumHCID 5360545—
LösungsmittelIsopropanolHCID 3776—
Produkt6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinolineHCID 1200162634%

Reaktionsschritte

(2-Amino-5-bromo-phenyl)-phenyl-methanone (10 g, 36 mmol), methanesulfonylacetone (7.4 g, 54 mmol) and sodium tetrachloroaureate(III) dihydrate (720 mg, 1.8 mmol) were heated at reflux in 2-propanol (100 mL) for 4.5 days. The resulting suspension was evaporated to dryness and the residue extracted with dichloromethane (2×), 1 N NaOH (2×), which removes excess of methanesulfonylacetone, and sat. NaCl (1×). The crude product was purified twice by chromatography in dichloromethane and then crystallized from dichloromethane/heptane by evaporation of dichloromethane. One obtained 4.6 g (33%) of beige crystals. MS: m/z=375/377 (M).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728142B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e1894e98006d45e997e4443d44c97654
Quellennotizuspto-grants-2010_06